Compositions comprising a fatty acid oil mixture and a surfactant, and methods and uses thereof

ABSTRACT

A preconcentrate comprising a fatty acid oil mixture that contains EPA and DHA, preferably in the form of ethyl ester or triglyceride, and at least one surfactant. The preconcentrates are capable of forming a self-nanoemulsifying drug delivery system, a self-microemulsifying drug delivery system or a self-emulsifying drug delivery system (SNEDDS, SMEDDS or SEDDS) in an aqueous solution. The application is also directed to a food supplement preconcentrate.

This application is a National Phase application based on InternationalPatent Application No. PCT/IB2010/000824 filed on Mar. 9, 2010, andclaims priority to U.S. Provisional Application No. 61/158,613, filed onMar. 9, 2009, U.S. Provisional Application No. 61/242,630, filed on Sep.15, 2009, U.S. Provisional Application No. 61/254,291, filed on Oct. 23,2009, and U.S. Provisional Application No. 61/254,293, filed on Oct. 23,2009, all of which are incorporated herein by reference in theirentireties.

The present disclosure relates generally to preconcentrates comprising afatty acid oil mixture and at least one surfactant, and methods of usethereof. The fatty acid oil mixture may comprise omega-3 fatty acids,such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) inethyl ester or triglyceride form. Further disclosed areself-nanoemulsifying drug delivery systems (SNEDDS),self-microemulsifying drug delivery systems (SMEDDS) andself-emulsifying drug delivery systems (SEDDS).

The preconcentrates presently disclosed may be administered, e.g., incapsule form, to a subject for therapeutic treatment and/or regulationof at least one health problem including, for example, irregular plasmalipid levels, cardiovascular functions, immune functions, visualfunctions, insulin action, neuronal development, hypertriglyceridemia,heart failure, and post myocardial infarction (MI). The presentdisclosure further relates to a method of increasing hydrolysis,solubility, bioavailability, absorption, and/or any combination thereof.

In humans, cholesterol and triglycerides are part of lipoproteincomplexes in the bloodstream and can be separated viaultracentrifugation into high-density lipoprotein (HDL),intermediate-density lipoprotein (IDL), low-density lipoprotein (LDL),and very-low-density lipoprotein (VLDL) fractions. Cholesterol andtriglycerides are synthesized in the liver, incorporated into VLDL, andreleased into the plasma. High levels of total cholesterol (total-C),LDL-C, and apolipoprotein B (a membrane complex for LDL-C and VLDL-C)promote human atherosclerosis and decreased levels of HDL-C and itstransport complex; apolipoprotein A is also associated with thedevelopment of atherosclerosis. Furthermore, cardiovascular morbidityand mortality in humans can vary directly with the level of total-C andLDL-C and inversely with the level of HDL-C. In addition, researchsuggests that non-HDL cholesterol is an indicator ofhypertriglyceridemia, vascular disease, atherosclerotic disease, andrelated conditions. In fact, NCEP ATP III specifies non-HDL cholesterolreduction as a treatment objective.

Omega-3 fatty acids may regulate plasma lipid levels, cardiovascular andimmune functions, insulin action, and neuronal development, and visualfunction. Marine oils, also commonly referred to as fish oils, are asource of omega-3 fatty acids, including eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA), have been found to regulate lipidmetabolism. Plant-based oils and microbial oils are also sources ofomega-3 fatty acids. Omega-3 fatty acids may have beneficial effects onthe risk factors for cardiovascular diseases, for example hypertensionand hypertriglyceridemia, and on the coagulation factor VII phospholipidcomplex activity. Omega-3 fatty acids may also lower serumtriglycerides, increase serum HDL cholesterol, lower systolic anddiastolic blood pressure and/or pulse rate, and may lower the activityof the blood coagulation factor VII-phospholipid complex. Further,omega-3 fatty acids are generally well-tolerated, without giving rise tosevere side effects.

Several formulations of omega-3 fatty acids have been developed. Forexample, one form of omega-3 fatty acid oil mixture is a concentrate ofprimary omega-3, long chain, polyunsaturated fatty acids from fish oilcontaining DHA and EPA, such as sold under the trademarkOmacor®/Lovaza™/Zodin®/Seacor®. See, for example, U.S. Pat. Nos.5,502,077, 5,656,667 and 5,698,594. In particular, each 1000 mg capsuleof Lovaza™ contains at least 90% omega-3 ethyl ester fatty acids (84%EPA/DHA); approximately 465 mg EPA ethyl ester and approximately 375 mgDHA ethyl ester.

Further, for example, EPA/DHA ethyl esters have also been used incompositions for delivery of therapeutic drugs. For instance, U.S. Pat.No. 6,284,268 (Cyclosporine Therapeutics Ltd.) describes aself-emulsifying microemulsion or emulsion preconcentrate pharmaceuticalcompositions containing an omega-3 fatty acid oil and poorly watersoluble therapeutic agent such as cyclosporine for oral administration.Cyclosporines are claimed to have additive or synergistic therapeuticeffects with omega-3 fatty acid oil. The '268 patent discloses greatersolubility and stability of cyclosporine formulations comprising omega-3fatty acid oils. WO 99/29300 (RTP Pharma) relates to self-emulsifyingfenofibrate formulations based on a hydrophobic component selected fromtriglyceride, diglyceride, monoglycerides, free fatty acids and fattyacids and derivatives thereof.

However, evidence suggests that long chain fatty acids and alcohols ofup to at least C₂₄ are reversibly interconverted. Enzyme systems existin the liver, fibroblasts, and the brain that convert fatty alcohols tofatty acids. In some tissues, fatty acids can be reduced back toalcohols. The carboxylic acid functional group of fatty acid moleculestargets binding, but this ionizable group may hinder the molecule fromcrossing the cell membranes, such as of the intestinal wall. As aresult, carboxylic acid functional groups are often protected as esters.The ester is less polar than the carboxylic acid, and may more easilycross the fatty cell membranes. Once in the bloodstream, the ester canbe hydrolyzed back to the free carboxylic acid by enzyme esterase in theblood. It may be possible that the plasma enzymes do not hydrolyze theester fast enough, however, and that the conversion of ester to freecarboxylic acid predominantly takes place in the liver. Ethyl esters ofpolyunsaturated fatty can also be hydrolyzed to free carboxylic acids invivo.

Thus, there remains a need in the art for compositions and/or methodsthat improve or enhance solubilization, digestion, bioavailabilityand/or absorption of omega-3 fatty acids in vivo, while maintaining theability to cross cell membranes.

It is to be understood that both the foregoing general description andthe following detailed description are exemplary and explanatory onlyand are not restrictive of the present disclosure, as claimed.

The present disclosure is further directed to a pharmaceuticalpreconcentrate comprising: a fatty acid oil mixture comprising at least75% eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), byweight of the fatty acid oil mixture, wherein the EPA and DHA are in aform chosen from ethyl ester and triglyceride; and at least onesurfactant.

The present disclosure is further directed to a pharmaceuticalpreconcentrate comprising: a fatty acid oil mixture comprising fromabout 80% to about 88% eicosapentaenoic acid (EPA) and docosahexaenoicacid (DHA), by weight of the fatty acid oil mixture, wherein the EPA andDHA are in ethyl ester form; and at least one surfactant chosen frompolysorbate 20, polysorbate 80, and mixtures thereof.

The present disclosure is further directed to a pharmaceuticalpreconcentrate comprising: a fatty acid oil mixture comprising fromabout 80% to about 88% eicosapentaenoic acid (EPA) and docosahexaenoicacid (DHA), by weight of the fatty acid oil mixture, wherein the EPA andDHA are in ethyl ester form; at least one surfactant chosen frompolysorbate 20, polysorbate 80, and mixtures thereof; and at least oneco-surfactant comprising ethanol.

The present disclosure is further directed to a self-nanoemulsifyingdrug delivery system (SNEDDS), self-microemulsifying drug deliverysystem (SMEDDS), or self-emulsifying drug delivery system (SEDDS)comprising a pharmaceutical preconcentrate comprising: a fatty acid oilmixture comprising from about 80% to about 88% eicosapentaenoic acid(EPA) and docosahexaenoic acid (DHA), by weight of the fatty acid oilmixture, wherein the EPA and DHA are in a form chosen from ethyl esterand triglyceride; and at least one surfactant; wherein thepreconcentrate forms an emulsion in an aqueous solution.

The present disclosure is further directed to a method of treating atleast one health problem in a subject in need thereof comprisingadministering to the subject a pharmaceutical preconcentrate comprising:a fatty acid oil mixture comprising at least 75% eicosapentaenoic acid(EPA) and docosahexaenoic acid (DHA), by weight of the fatty acid oilmixture, wherein the EPA and DHA are in a form chosen from ethyl esterand triglyceride; and at least one surfactant; wherein the at least onehealth problem is chosen from irregular plasma lipid levels,cardiovascular functions, immune functions, visual functions, insulinaction, neuronal development, heart failure, and post myocardialinfarction.

The present disclosure is further directed to a food supplementpreconcentrate or nutritional supplement preconcentrate comprising: afatty acid oil mixture comprising from about 25% to about 75%eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), by weight ofthe fatty acid oil mixture, wherein the EPA and DHA are in a form chosenfrom ethyl ester and triglyceride; and at least one surfactant.

The present disclosure is further directed to a method for enhancing atleast one parameter chosen from hydrolysis, solubility, bioavailability,absorption, and combinations thereof of eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA) comprising combining: a fatty acid oilmixture comprising EPA and DHA in a form chosen from ethyl ester andtriglyceride; and at least one surfactant; wherein the fatty acid oilmixture and the at least one surfactant form a preconcentrate.

The present disclosure is further directed to a method of regulating atleast one health problem in a subject in need thereof comprisingadministering to the subject a supplement preconcentrate comprising: afatty acid oil mixture comprising from about 25% to about 75%eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), by weight ofthe fatty acid oil mixture, wherein the EPA and DHA are in a form chosenfrom ethyl ester and triglyceride; and at least one surfactant; whereinthe at least one health problem is chosen from irregular plasma lipidlevels, cardiovascular functions, immune functions, visual functions,insulin action, neuronal development, heart failure, and post myocardialinfarction.

The present disclosure is further directed to a food supplement ornutritional supplement preconcentrate comprising; a fatty acid oilmixture comprising from about 25% to about 75% eicosapentaenoic acid(EPA) and docosahexaenoic acid (DHA), by weight of the fatty acid oilmixture, wherein the EPA and DHA are in a form chosen from ethyl esterand triglyceride; and at least one surfactant for the regulation of atleast one health problem chosen from irregular plasma lipid levels,cardiovascular functions, immune functions, visual functions, insulinaction, neuronal development, heart failure, and post myocardialinfarction.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of Omacor®.

FIG. 2 shows the percent recovery of EPA+DHA at different time-pointsfor Omacor®.

FIG. 3 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for Omacor®.

FIG. 4 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of preconcentrate A.

FIG. 5 shows the percent recovery of EPA+DHA at different time-pointsfor preconcentrate A.

FIG. 6 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for preconcentrate A.

FIG. 7 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of preconcentrate B.

FIG. 8 shows the percent recovery of EPA+DHA at different time-pointsfor preconcentrate B.

FIG. 9 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for preconcentrate B.

FIG. 10 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of preconcentrate C.

FIG. 11 shows the percent recovery of EPA+DHA at different time-pointsfor preconcentrate C.

FIG. 12 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for preconcentrate C.

FIG. 13 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of preconcentrate D.

FIG. 14 shows the percent recovery of EPA+DHA at different time-pointsfor preconcentrate D.

FIG. 15 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for preconcentrate D.

FIG. 16 shows the disappearance of EPA-EE and DHA-EE and the appearanceof EPA-FA and DHA-FA during lipolysis of preconcentrate E.

FIG. 17 shows the percent recovery of EPA+DHA at different time-pointsfor preconcentrate E.

FIG. 18 shows the percent lipolysis of EPA-EE, DHA-EE and total K85EE atdifferent time points for preconcentrate E.

DESCRIPTION

Particular aspects of the disclosure are described in greater detailbelow. The terms and definitions as used in the present application andas clarified herein are intended to represent the meaning within thepresent disclosure. The patent and scientific literature referred toherein and referenced above is hereby incorporated by reference. Theterms and definitions provided herein control, if in conflict with termsand/or definitions incorporated by reference.

The singular forms “a,” “an,” and “the” include plural reference unlessthe context dictates otherwise.

The terms “approximately” and “about” mean to be nearly the same as areferenced number or value. As used herein, the terms “approximately”and “about” should be generally understood to encompass±10% of aspecified amount, frequency or value.

The terms “administer,” “administration” or “administering” as usedherein refer to (1) providing, giving, dosing and/or prescribing byeither a health practitioner or his authorized agent or under hisdirection a preconcentrate according to the disclosure, and (2) puttinginto, taking or consuming by the patient or person himself or herself, apreconcentrate according to the disclosure.

The present disclosure provides for pharmaceutical and supplementpreconcentrates comprising a fatty acid oil mixture and at least onesurfactant, and methods of use thereof. The preconcentrates of thepresent disclosure can produce dispersions of low or very low meanparticle size when mixed with an aqueous medium. Such dispersions can becharacterized as nanoemulsions, microemulsions, or emulsions. Forexample, upon delivery, the preconcentrates are thought to producedispersions with gastric or other physiological fluids generatingself-nanoemulsifying drug delivery systems (SNEDDS),self-microemulsifying drug delivery systems (SMEDDS), or selfemulsifying drug delivery systems (SEDDS).

Fatty Acid Oil Mixture

Compositions of the present disclosure comprise at least one fatty acidoil mixture comprising eicosapentaenoic acid (EPA) and docosahexaenoicacid (DHA). As used herein, the term “fatty acid oil mixture” includesfatty acids, such as unsaturated (e.g., monounsaturated,polyunsaturated) or saturated fatty acids, as well aspharmaceutically-acceptable esters, free acids, mono-, di- andtriglycerides, derivatives, conjugates, precursors, salts, and mixturesthereof. In at least one embodiment, the fatty acid oil mixturecomprises fatty acids, such as omega-3 fatty acids, in a form chosenfrom ethyl ester and triglyceride.

The term “omega-3 fatty acids” includes natural and synthetic omega-3fatty acids, as well as pharmaceutically-acceptable esters, free acids,triglycerides, derivatives, conjugates (see, e.g., Zaloga et al., U.S.Patent Application Publication No. 2004/0254357, and Horrobin et al.,U.S. Pat. No. 6,245,811, each hereby incorporated by reference),precursors, salts, and mixtures thereof. Examples of omega-3 fatty acidoils include, but are not limited to, omega-3 polyunsaturated,long-chain fatty acids such as eicosapentaenoic acid (EPA),docosahexaenoic acid (DHA), α-linolenic acid (ALA), heneicosapentaenoicacid (HPA), docosapentaenoic acid (DPA), eicosatetraenoic acid (ETA),eicosatrienoic acid (ETE), and octadecatetraenoic acid (i.e.,stearidonic acid, STA); esters of omega-3 fatty acids with glycerol suchas mono-, di- and triglycerides; and esters of the omega-3 fatty acidsand a primary, secondary and/or tertiary alcohol, such as, for example,fatty acid methyl esters and fatty acid ethyl esters. The omega-3 fattyacids, esters, triglycerides, derivatives, conjugates, precursors, saltsand/or mixtures thereof according to the present disclosure can be usedin their pure form and/or as a component of an oil, for example, asmarine oil (e.g., fish oil and purified fish oil concentrates), algaeoils, microbial oils and plant-based oils.

In some embodiments of the present disclosure, the fatty acid oilmixture comprises EPA and DHA. Further for example, the fatty acid oilmixture comprises EPA and DHA in a form chosen from ethyl ester andtriglyceride.

The fatty acid oil mixture of the present disclosure may furthercomprise at least one fatty acid other than EPA and DHA. Examples ofsuch fatty acids include, but are not limited to, omega-3 fatty acidsother than EPA and DHA and omega-6 fatty acids. For example, in someembodiments of the present disclosure, the fatty acid oil mixturecomprises at least one fatty acid other than EPA and DHA chosen fromα-linolenic acid (ALA), heneicosapentaenoic acid (HPA), docosapentaenoicacid (DPA), eicosatetraenoic acid (ETA), eicosatrienoic acid (ETE), andstearidonic acid (STA). In some embodiments, the at least one fatty acidother than EPA and DHA is chosen from linoleic acid, gamma-linolenicacid (GLA), arachidonic acid (AA), docosapentaenoic acid (i.e., osbondacid), and mixtures thereof. In some embodiments, the at least one fattyacid other than EPA and DHA is in a form chosen from ethyl ester andtriglyceride.

Examples of further fatty acids, or mixtures thereof (fatty acid oilmixtures) encompassed by the present disclosure include, but are notlimited to, the fatty acids defined in the European PharamacopoeiaOmega-3 Ethyl Esters 90 and purified marine oils, the EuropeanPharamacopoeia Omega-3 Acid Triglycerides, the European PharamacopoeiaOmega-3 acid Ethyl Esters 60, the European Pharmacopoeia Fish Oil Richin Omega-3 Acids monograph, and/or for instance, the USP fish oilmonograph.

Commercial examples of fatty acid oil mixtures comprising differentfatty acids suitable for the present disclosure include, but are notlimited to: Incromega™ omega-3 marine oil concentrates such asIncromega™ TG7010 SR, Incromega™ E7010 SR, Incromega™ TG6015, Incromega™EPA500TG SR, Incromega™ E400200 SR, Incromega™ E4010, Incromega™DHA700TG SR, Incromega™ DHA700E SR, Incromega™ DHA500TG SR, Incromega™TG3322 SR, Incromega™ E3322 SR, Incromega™ TG3322, Incromega™ E3322,Incromega™ Trio TG/EE (Croda International PLC, Yorkshire, England);EPAX6000FA, EPAX5000TG, EPAX4510TG, EPAX2050TG, EPAX7010EE, EPAX5500EE,EPAX5500TG, EPAX5000EE, EPAX5000TG, EPAX6000EE, EPAX6000TG, EPAX6000FA,EPAX6500EE, EPAX6500TG, EPAX4510TG, EPAX1050TG, EPAX2050TG, EPAX 7010TG,EPAX7010EE, EPAX6015TG/EE, EPAX4020TG, and EPAX4020EE (EPAX is awholly-owned subsidiary of Norwegian company Austevoll Seafood ASA);Omacor®/Lovaza™/Zodin®/Seacor® finished pharmaceutical product, K85EE,and AGP 103 (Pronova BioPharma Norge AS); MEG-3® EPA/DHA fish oilconcentrates (Ocean Nutrition Canada); DHA FNO “Functional NutritionalOil” and DHA CL “Clear Liquid” (Lonza); Superba™ Krill Oil (Aker);omega-3 products comprising DHA produced by Martek; Neptune krill oil(Neptune); cod-liver oil products and anti-reflux fish oil concentrate(TG) produced by Møllers; Lysi Omega-3 Fish oil; Seven Seas Triomega®Cod Liver Oil Blend (Seven Seas); Fri Flyt Omega-3 (Vesterålens); andEpadel (Mochida). Those commercial embodiments provide for variousomega-3 fatty acids, combinations, and other components as a result ofthe transesterification process or method of preparation in order toobtain the omega-3 fatty acid(s) from various sources, such as marine,algae, microbial, and plant-based sources.

In some embodiments of the present disclosure, the fatty acid oilmixture comprises at least one fatty acid derivative, such as analpha-substituted omega-3 fatty acid derivative. The at least one alphasubstituted omega-3 fatty acid derivative may be substituted, forexample, at the second carbon atom from the functional group of theomega-3 fatty acid with at least one substituent chosen from hydrogen,hydroxyl groups, alkyl groups, such as C₁-C₃ alkyl groups, and alkoxygroups. In one embodiment of the present disclosure, the at least onealpha-substituted omega-3 fatty acid derivative is chosen frommono-substituted and di-substituted fatty acids. In one embodiment, theat least one alpha substituted omega-3 fatty acid derivative is chosenfrom alpha-substituted C₁₄-C₂₄ alkenes having 2 to 6 double bonds. Inanother embodiment, the at least one alpha-substituted omega-3 fattyacid derivative is chosen from alpha-substituted C₁₄-C₂₄ alkenes having5 or 6 double bonds in cis configuration.

In some embodiments, the fatty acid oil mixture comprises EPA and/or DHAin a form of an alpha-substituted fatty acid derivative. For example, inone embodiment, the fatty acid oil mixture comprises EPA in a form of analpha-substituted derivative. In another embodiment, the fatty acid oilmixture comprises DHA in a form of an alpha-substituted derivative. Inyet another embodiment, the fatty acid oil mixture comprises EPA and DHAin a form of an alpha-substituted derivative.

In some embodiments, the fatty acid oil mixture comprises EPA and DHA,and further comprises at least one alpha-substituted omega-3 fatty acidderivative. For example, in some embodiments, the fatty acid oil mixturecomprises EPA and DHA, and at least one of EPA and DHA in a form of analpha-substituted derivative.

In another embodiment, the EPA and DHA of the fatty acid oil mixture isat least one alpha-substituted omega-3 fatty acid derivative.

The fatty acid oil mixture according to the present disclosure may bederived from animal oils and/or non-animal oils. In some embodiments ofthe present disclosure, the fatty acid oil mixture is derived from atleast one oil chosen from marine oil, algae oil, plant-based oil, andmicrobial oil. Marine oils include, for example, fish oil, krill oil,and lipid composition derived from fish. Plant-based oils include, forexample, flaxseed oil, canola oil, mustard seed oil, and soybean oil.Microbial oils include, for example, products by Martek. In at least oneembodiment of the present disclosure, the fatty acid oil mixture isderived from a marine oil, such as a fish oil. In at least oneembodiment, the marine oil is a purified fish oil.

In some embodiments of the present disclosure, the fatty acids, such asomega-3 fatty acids, of the fatty acid oil mixture are esterified, suchas alkyl esters, such as ethyl ester. In other embodiments, the fattyacids are chosen from mono-, di-, and triglycerides.

In some embodiments, the fatty acid oil mixture is obtained by atransesterification of the body oil of a fat fish species coming from,for example, anchovy or tuna oil, and subsequent physico-chemicalpurification processes, including urea fractionation followed bymolecular distillation. In some embodiments, the crude oil mixture mayalso be subjected to a stripping process for decreasing the amount ofenvironmental pollutants and/or cholesterol before thetransesterification.

In another embodiment, the fatty acid oil mixture is obtained by usingsupercritical CO₂ extraction or chromatography techniques, for exampleto up-concentrate primary EPA and DHA from fish oil concentrates.

In some embodiments of the present disclosure, at least one of theomega-3 fatty acids of the fatty acid oil mixture has a cisconfiguration. Examples include, but are not limited to,(all-Z)-9,12,15-octadecatrienoic acid (ALA),(all-Z)-6,9,12,15-octadecatetraenoic acid (STA),(all-Z)-11,14,17-eicosatrienoic acid (ETE),(all-Z)-5,8,11,14,17-eicosapentaenoic acid (EPA),(all-Z)-4,7,10,13,16,19-docosahexaenoic acid (DHA),(all-Z)-8,11,14,17-eicosatetraenoic acid (ETA),(all-Z)-7,10,13,16,19-docosapentaenoic acid (DPA),(all-Z)-6,9,12,15,19-heneicosapentaenoic acid (HPA);(all-Z)-5,8,11,14-eicosatetraenoic acid,(all-Z)-4,7,10,13,16-docosapentaenoic acid (osbond acid),(all-Z)-9,12-octadecadienoic acid (linoleic acid),(all-Z)-5,8,11,14-eicosatetraenoic acid (AA),(all-Z)-6,9,12-octadecatrienoic acid (GLA); (Z)-9-octadecenoic acid(oleic acid), 13(Z)-docosenoic acid (erucic acid),(R—(Z))-12-hydroxy-9-octadecenoic acid (ricinoleic acid).

In some embodiments of the present disclosure, the weight ratio ofEPA:DHA of the fatty acid oil mixture ranges from about 1:10 to about10:1, from about 1:8 to about 8:1, from about 1:6 to about 6:1, fromabout 1:5 to about 5:1, from about 1:4 to about 4:1, from about 1:3 toabout 3:1, or from about 1:2 to about 2:1. In at least one embodiment,the weight ratio of EPA:DHA of the fatty acid oil mixture ranges fromabout 1:2 to about 2:1. In at least one embodiment, the weight ratio ofEPA:DHA of the fatty acid oil mixture ranges from about 1:1 to about2:1. In at least one embodiment, the weight ratio of EPA:DHA of thefatty acid oil mixture ranges from about 1:2 to about 1:3.

Pharmaceutical

In some embodiments of the present disclosure, the fatty acid oilmixture acts as an active pharmaceutical ingredient (API). For example,the present disclosure provides for a pharmaceutical compositioncomprising a fatty acid oil mixture and at least one surfactant. In someembodiments, the fatty acid oil mixture is present in apharmaceutically-acceptable amount. As used herein, the term“pharmaceutically-effective amount” means an amount sufficient to treat,e.g., reduce and/or alleviate the effects, symptoms, etc., at least onehealth problem in a subject in need thereof. In at least someembodiments of the present disclosure, the fatty acid oil mixture doesnot comprise an additional active agent.

Where the preconcentrate is a pharmaceutical preconcentrate, the fattyacid oil mixture comprises at least 75% EPA and DHA by weight of thefatty acid oil mixture. In some embodiments, the fatty acid oil mixturecomprises at least 80% EPA and DHA by weight of the fatty acid oilmixture, such as at least 85%, at least 90%, or at least 95%, by weightof the fatty acid oil mixture. In some embodiments, the fatty acid oilmixture comprises about 80% EPA and DHA by weight of the fatty acid oilmixture, such as about 85%, about 90%, about 95%, or any number inbetween, by weight of the fatty acid oil mixture.

For example, in some embodiments, the fatty acid oil mixture comprisesfrom about 75% to about 95% EPA and DHA by weight of the fatty acid oilmixture, such as from about 75% to about 90%, from about 75% to about88%, from about 75% to about 85%, from about 75% to about 80%, fromabout 80% to about 95%, from about 80% to about 90%, from about 80% toabout 85%, from about 85% to about 95%, from about 85% to about 90%, andfurther for example, from about 90% to about 95% EPA and DHA, by weightof the fatty acid oil mixture, or any number in between. In at least oneembodiment, the fatty acid oil mixture comprises from about 80% to about85% EPA and DHA, by weight of the fatty acid oil mixture, such as fromabout 80% to about 88%, such as about 84%, by weight of the fatty acidoil mixture.

In some embodiments, the fatty acid oil mixture comprises at least 95%of EPA or DHA, or EPA and DHA, by weight of the fatty acid oil mixture,wherein the EPA and DHA are in ethyl ester form.

In a further embodiment, the fatty acid oil mixture may comprise otheromega-3 fatty acids. For example, the present disclosure encompasses atleast 90% omega-3 fatty acids, by weight of the fatty acid oil mixture.

In one embodiment, for example, the fatty acid oil mixture comprisesfrom about 75% to about 88% EPA and DHA, by weight of the fatty acid oilmixture, wherein the EPA and DHA are in ethyl ester form; wherein thefatty acid oil mixture comprises at least 90% of omega-3 fatty acids inethyl ester form, by weight of the fatty acid oil mixture.

In another embodiment, the fatty acid oil mixture comprises from about75% to about 88% EPA and DHA, by weight of the fatty acid oil mixture,wherein the EPA and DHA are in ethyl ester form; wherein the fatty acidoil mixture comprises at least 90% of omega-3 fatty acids in ethyl esterform, by weight of the fatty acid oil mixture, and wherein the fattyacid oil mixture comprises α-linolenic acid (ALA).

In one embodiment, the fatty acid oil mixture comprises from about 80%to about 88% EPA and DHA by weight of the fatty acid oil mixture,wherein the EPA and DHA are in ethyl ester form, and further comprisesdocosapentaenoic acid (DPA) in ethyl ester form.

In another embodiment, the fatty acid oil mixture comprises from about80% to about 88% EPA and DHA by weight of the fatty acid oil mixture,wherein the EPA and DHA are in ethyl ester form, and further comprisesfrom about 1% to about 4% (all-Zomega-3)-6,9,12,15,18-heneicosapentaenoic acid (HPA) in ethyl esterform, by weight of the fatty acid oil mixture.

In another embodiment, the fatty acid oil mixture comprises from about80% to about 88% EPA and DHA by weight of the fatty acid oil mixture,wherein the EPA and DHA are in ethyl ester form; and from 1% to about 4%fatty acid ethyl esters other than EPA and DHA, by weight of the fattyacid oil mixture, wherein the fatty acid ethyl esters other than EPA andDHA have C₂₀, C₂₁, or C₂₂ carbon atoms.

In one embodiment, the fatty acid oil mixture may comprise K85EE or AGP103 (Pronova BioPharma Norge AS). In another embodiment, the fatty acidoil mixture may comprise K85TG (Pronova BioPharma Norge AS).

EPA and DHA Products

In at least one embodiment, the fatty acid oil mixture comprises atleast 75% EPA and DHA by weight of the fatty acid oil mixture, of whichat least 95% is EPA. In another embodiment, the fatty acid oil mixturecomprises at least 80% EPA and DHA by weight of the fatty acid oilmixture, of which at least 95% is EPA. In yet another embodiment, thefatty acid oil mixture comprises at least 90% EPA and DHA by weight ofthe fatty acid oil mixture, of which at least 95% is EPA.

In another embodiment, the fatty acid oil mixture comprises at least 75%EPA and DHA by weight of the fatty acid oil mixture, of which at least95% is DHA. For example, in one embodiment, the fatty acid oil mixturecomprises at least 80% EPA and DHA by weight of the fatty acid oilmixture, of which at least 95% is DHA. In another embodiment, the fattyacid oil mixture comprises at least 90% EPA and DHA by weight of thefatty acid oil mixture, of which at least 95% is DHA.

Supplement

The present disclosure further provides a food supplement or anutritional supplement comprising a fatty acid oil mixture and at leastone surfactant, wherein the fatty acid oil mixture comprises less than75% EPA and DHA by weight of the fatty acid oil mixture. In someembodiments, for example, the fatty acid oil comprises less than 70% EPAand DHA by weight of the fatty acid oil mixture, such as less than 65%,less than 60%, less than 55%, less than 50%, less than 45%, less than40%, or even less than 35% by weight of the fatty acid oil mixture.

In some embodiments, the fatty acid oil mixture comprises from about 25%to about 75% EPA and DHA by weight of the fatty acid oil mixture, suchas from about 30% to about 75%, from about 30% to about 70%, from about30% to about 65%, from about 30% to about 55%, from about 30% to about50%, from about 30% to about 45%, from about 30% to about 40%, andfurther for example, from about 30% to about 35% EPA and DHA, by weightof the fatty acid oil mixture.

In some embodiments of the present disclosure, the fatty acids, such asomega-3 fatty acids, of the fatty acid oil mixture are esterified, suchas alkyl esters. The alkyl esters may include, but are not limited to,ethyl, methyl, propyl, and butyl esters, and mixtures thereof. In otherembodiments, the fatty acids are chosen from mono-, di-, andtriglycerides. For example, the fatty acid oil mixture comprises fromabout 25% to about 75% EPA and DHA by weight of the fatty acid oilmixture in a form chosen from methyl ester, ethyl ester, andtriglyceride.

Surfactant/Preconcentrate

The present disclosure further provides for a preconcentratecomposition. As used herein, the term “preconcentrate” refers to acomposition comprising a fatty acid oil mixture and at least onesurfactant.

A surfactant may, for example, lower the surface tension of a liquid orthe surface tension between two liquids. For example, surfactantsaccording to the present disclosure may lower the surface tensionbetween the fatty acid oil mixture and an aqueous solution.

Chemically speaking, surfactants are molecules with at least onehydrophilic part and at least one hydrophobic (i.e., lipophilic) part.Surfactant properties may be reflected in the hydrophilic-lipophilicbalance (HLB) value of the surfactant, wherein the HLB value is ameasure of the degree of hydrophilic versus lipophilic properties of asurfactant. The HLB value normally ranges from 0 to 20, where a HLBvalue of 0 represents high hydrophilic character, and a HLB of 20represents high lipophilic character. Surfactants are often used incombination with other surfactants, wherein the HLB values are additive.The HLB value of surfactant mixtures may be calculated as follows:HLB_(A)(fraction of surfactant A)+HLB_(B)(fraction of surfactantB)=HLB_(A+B mixture)

Surfactants are generally classified as ionic surfactants, e.g., anionicor cationic surfactants, and nonionic surfactants. If the surfactantcontains two oppositely charged groups, the surfactant is named azwitterionic surfactant. Other types of surfactants include, forexample, phospholipids.

In at least one embodiment of the present disclosure, the preconcentratecomprises at least one surfactant chosen from nonionic, anionic,cationic, and zwitterionic surfactants.

Non-limiting examples of nonionic surfactants suitable for the presentdisclosure are mentioned below.

Pluronic® surfactants are nonionic copolymers composed of a centralhydrophobic polymer (polyoxypropylene(poly(propylene oxide))) with ahydrophilic polymer (polyoxyethylene(poly(ethylene oxide))) on eachside. Various commercially-available Pluronic® products are listed inTable 1.

TABLE 1 Examples of Pluronic ® surfactants. Average Molecular TypeWeight (D) HLB Value Pluronic ® L-31 Non-ionic 1100 1.0-7.0 Pluronic ®L-35 Non-ionic 1900 18.0-23.0 Pluronic ® L-61 Non-ionic 2000 1.0-7.0Pluronic ® L-81 Non-ionic 2800 1.0-7.0 Pluronic ® L-64 Non-ionic 290012.0-18.0 Pluronic ® L-121 Non-ionic 4400 1.0-7.0 Pluronic ® P-123Non-ionic 5800 7-9 Pluronic ® F-68 Non-ionic 8400 >24 Pluronic ® F-108Non-ionic 14600 >24

Brij® are nonionic surfactants comprising polyethylene ethers. Variouscommercially-available Brij® products are listed in Table 2.

TABLE 2 Examples of Brij ® surfactants. HLB Type Compound Value Brij ®30 Non-ionic Polyoxyethylene(4) lauryl ether 9.7 Brij ® 35 Non-ionicpolyoxyethylene (23) lauryl ether 16.9 Brij ® 52 Non-ionicPolyoxyethylene (2) cetyl ether 5.3 Brij ® 56 Non-ionic Polyoxyethylene(10) cetyl ether 12.9 Brij ® 58 Non-ionic Polyoxyethylene (20) cetylether 15.7 Brij ® 72 Non-ionic polyoxyethylene (2) stearyl ether 4.9Brij ® 76 Non-ionic polyoxyethylene (10) stearyl ether 12.4 Brij ® 78Non-ionic polyoxyethylene (20) stearyl ether 15.3 Brij ® 92V Non-ionicPolyoxyethylene (2) oleyl ether 4.9 Brij ® 93 Non-ionic Polyoxyethylene(2) oleyl ether 4 Brij ® 96V Non-ionic polyethylene glycol oleyl ether12.4 Brij ® 97 Non-ionic Polyoxyethylene (10) oleyl ether 12 Brij ® 98Non-ionic Polyoxyethylene (20) oleyl ether 15.3 Brij ® 700 Non-ionicpolyoxyethylene (100) stearyl ether 18

Span® are nonionic surfactants comprising sorbitan esters. Span® isavailable from different sources including Aldrich. Variouscommercially-available Span® products are listed in Table 3.

TABLE 3 Examples of Span ® surfactants. Type Compound HLB Value Span ®20 Non-ionic sorbitan monolaurate 8.6 Span ® 40 Non-ionic sorbitanmonopalmitate 6.7 Span ® 60 Non-ionic sorbitan monostearate 4.7 Span ®65 Non-ionic sorbitan tristearate 2.1 Span ® 80 Non-ionic sorbitanmonooleate 4.3 Span ® 85 Non-ionic Sorbitan trioleate 1.8

Tween® (polysorbates) are nonionic surfactants comprisingpolyoxyethylene sorbitan esters. Various commercially-available Tween®products are listed in Table 4.

TABLE 4 Examples of Tween ® surfactants. Type Compound HLB Value Tween ®20 Non-ionic polyoxyethylene (20) 16.0 sorbitan monolaurate Tween ® 40Non-ionic polyoxyethylene (20) 15.6 sorbitan monopalmitate Tween ® 60Non-ionic polyoxyethylene sorbitan 14.9 monostearate Tween ® 65Non-ionic polyoxyethylene sorbitan 10.5 tristearate Tween ® 80 Non-ionicpolyoxyethylene(20) 15.0 sorbitan monooleate Tween ® 85 Non-ionicpolyoxyethylene sorbane 11.0 trioleate

Myrj® are nonionic surfactants comprising polyoxyethylene fatty acidesters. Various commercially-available Myrj® products are listed inTable 5.

TABLE 5 Examples of Myrj ® surfactants. Type Compound HLB Value Myrj ®45 Non-ionic polyoxyethylene monostearate 11.1 Myrj ® 49 Non-ionicpolyoxyethylene monostearate 15.0 Myrj ® 52 Non-ionic polyoxyethylenemonostearate 16.9 Myrj ® 53 Non-ionic polyoxyethylene monostearate 17.9

Cremophor® are nonionic surfactants. Various commercially-availableCremophor® products are listed in Table 6.

TABLE 6 Examples of Cremophor ® surfactants. Type Compound HLB ValueCremophor ® REL Non-ionic polyoxyethylated  2-14 castor oil Cremophor ®RH40 Non-ionic hydrogenated 14-16 polyoxyethylated castor oilCremophor ® RH60 Non-ionic hydrogenated 15-17 polyoxyethylated castoroil Cremophor ® RO Non-ionic hydrogenated 16.1 polyoxyethylated castoroil

According to the present disclosure, other exemplary nonionicsurfactants include, but are not limited to, diacetyl monoglycerides,diethylene glycol monopalmitostearate, ethylene glycolmonopalmitostearate, glyceryl behenate, glyceryl distearate, glycerylmonolinoleate, glyceryl mono-oleate, glyceryl monostearate, macrogolcetostearyl ether such as cetomacrogol 1000 and polyoxy 20 cetostearylether, macrogol 15 hydroxystearate, macrogol lauril ethers such aslaureth 4 and lauromacrogol 400, macrogol monomethyl ethers, macrogololeyl ethers such as polyoxyl 10 oleyl ether, macrogol stearates such aspolyoxyl 40 stearate, menfegol, mono and diglycerides, nonoxinols suchas nonoxinol-9, nonoxinol-10 and nonoxinol-11, octoxinols such asoctoxinol 9 and oxtoxinol 10, polyoxamers such as polyoxalene,polyoxamer 188, polyoxamer 407, polyoxyl castor oil such as polyoxyl 35castor oil, polyoxyl hydrogenated castor oil such as polyoxyl 40hydrogenated castor oil, propylene glycol diacetate, propylene glycollaurates such as propylene glycol dilaurate and propylene glycolmonolaurate. Further examples include propylene glycolmonopalmitostearate, quillaia, sorbitan esters, and sucrose esters.

Anionic surfactants suitable for the present disclosure include, forexample, salts of perfluorocarboxylic acids and perfluorosulphonic acid,alkyl sulphate salts such as sodium dodecyl sulphate and ammonium laurylsulphate, sulphate ethers such as sodium lauryl ether sulphate, andalkyl benzene sulphonate salts.

Cationic surfactants suitable for the present disclosure include, forexample, quaternary ammonium compounds such as benzalkonium chloride,cetylpyridinium chlorides, benzethonium chlorides, and cetyltrimethylammonium bromides or other trimethylalkylammonium salts.

Zwitterionic surfactants include, but are limited to, for exampledodecyl betaines, coco amphoglycinates and cocamidopropyl betaines.

In some embodiments of the present disclosure, the surfactant maycomprise a phospholipid, derivative thereof, or analogue thereof. Suchsurfactants may, for example, be chosen from natural, synthetic, andsemisynthetic phospholipids, derivatives thereof, and analogues thereof.Phospholipids may be “natural” or from a marine origin chosen from,e.g., phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine,and phosphatidylinosytol. The fatty acid moiety may be chosen from 14:0,16:0, 16: 1n-7, 18:0, 18:1n-9, 18:1n-7, 18:2n-6, 18:3n-3, 18:4n-3,20:4n-6, 20:5n-3, 22:5n-3 and 22:6n-3, or any combinations thereof. Inone embodiment, the fatty acid moiety is chosen from palmitic acid, EPAand DHA. Exemplary phospholipids surfactants includephosphatidylcholines with saturated, unsaturated and/or polyunsaturatedlipids such as dioleoylphosphatidylcholine,dipentadecanoylphosphatidylcholine, dilauroylphosphatidylcholine,dimyristoylphosphatidylcholine, dipalmitoylphosphatidylcholine,distearoylphosphatidylcholine, dieicopentaenoyl(EPA)choline,didocosahexaenoyl(DHA)choline, phosphatidylethanolamines,phosphatidylglycerols, phosphatidylserines and phosphatidylinositols.Other exemplary phospholipid surfactants include soybean lecithin, egglecithin, diolelyl phosphatidylcholine, distearoyl phosphatidylglycerol, PEG-ylated phospholipids, and dimyristoyl phosphatidylcholine.

Other exemplary surfactants suitable for the present disclosure arelisted in Table 7.

TABLE 7 Other surfactants Surfactant Type HBL Value Ethylene glycoldistearate Nonionic 1.5 Glyceryl monostearate Nonionic 3.3 Propyleneglycol monostearate Nonionic 3.4 Glyceryl monostearate Nonionic 3.8Diethylene glycol monolaurate Nonionic 6.1 Acacia Anionic 8.0Cetrimonium bromide Cationic 23.3 Cetylpyridinium chloride Cationic 26.0Polyoxamer 188 Nonionic 29.0 Sodium lauryl sulphate Anionic 40

In some embodiments of the present disclosure, the at least onesurfactant does not comprise Labrasol, Cremophor RH40, or thecombination of Cremophor and Tween-80.

In some embodiments, the at least one surfactant has ahydrophilic-lipophilic balance (HLB) of less than about 10, such as lessthan about 9, or less than about 8.

Co-Surfactant

In some embodiments, compositions of the present disclosure furthercomprise at least one co-surfactant. As used herein the term“co-surfactant” means a substance added to the preconcentrate incombination with the at least one surfactant to affect, e.g., increaseor enhance, emulsification and/or stability of the preconcentrate, forexample to aid in forming an emulsion. In some embodiments, the at leastone co-surfactant is hydrophilic. In some embodiments, the at least oneco-surfactant is not in free acid form.

Examples of co-surfactants suitable for the present disclosure include,but are not limited to, short chain alcohols comprising from 1 to 6carbons (e.g., ethanol), benzyl alcohol, alkane diols and triols (e.g.,propylene glycol, glycerol, polyethylene glycols such as PEG and PEG400), glycol ethers such as tetraglycol and glycofurol (e.g.,tetrahydrofurfuryl PEG ether), pyrrolidine derivatives such asN-methylpyrrolidone (e.g., Pharmasolve®) and 2-pyrrolidone (e.g.,Soluphor® P), and bile salts, for example sodium deoxycholate. Furtherexamples include ethyl oleate.

In some embodiments, the at least one co-surfactant comprises from about1% to about 10%, by weight relative to the weight of the preconcentrate.

Solvent

In some embodiments, compositions according to the present disclosure,such as the preconcentrate, further comprises at least one solvent. Asused herein, the term “solvent” means a substance added to thepreconcentrate to affect and/or alter the consistency of thepreconcentrate, for example in an aqueous solution. In some embodiments,the solvent is hydrophilic. Hydrophilic solvents suitable for thepresent disclosure include, but are not limited to, alcohols, includingwater-miscible alcohols, such as absolute ethanol and/or glycerol, andglycols, for example glycols obtainable from an oxide such as ethyleneoxide, such as 1,2-propylene glycol. Other non-limiting examples includepolyols, such as polyalkylene glycol, e.g., poly(C₂₋₃)alkylene glycolsuch as polyethylene glycol. In at least one embodiment, the at leastone solvent is a pharmaceutically-acceptable solvent.

In some embodiments of the present disclosure, the preconcentratecomprises at least one substance that acts both as a co-surfactant and asolvent, for example an alcohol such as ethanol. In other embodiments,the preconcentrate comprises at least one co-surfactant and at least onesolvent that are different substances. For example, in some embodimentsthe preconcentrate comprises ethanol as the co-surfactant and glycerolas the solvent.

In some embodiments of the present disclosure, the preconcentrate is apharmaceutical preconcentrate comprising a fatty acid oil mixturecomprising at least 75% eicosapentaenoic acid (EPA) and docosahexaenoicacid (DHA), by weight of the fatty acid oil mixture, wherein the EPA andDHA are in a form chosen from ethyl ester and triglyceride; and at leastone surfactant.

In one embodiment, the pharmaceutical preconcentrate comprises: a fattyacid oil mixture comprising at least 95% of EPA ethyl ester, DHA ethylester, or mixtures thereof, by weight of the fatty acid oil mixture; anda least one surfactant chosen from polysorbate 20, polysorbate 80, andmixtures thereof.

In another embodiment, the pharmaceutical preconcentrate comprises: afatty acid oil mixture comprising from about 80% to about 88% EPA andDHA by weight of the fatty acid oil mixture, wherein the EPA and DHA arein ethyl ester form; and at least one surfactant chosen from polysorbate20, polysorbate 80, and mixtures thereof; wherein the at least onesurfactant comprises less than 40%, by weight relative to the weight ofthe preconcentrate.

In another embodiment, the pharmaceutical preconcentrate comprises: afatty acid oil mixture comprising from about 80% to about 88% EPA andDHA by weight of the fatty acid oil mixture, wherein the EPA and DHA arein ethyl ester form; and at least one surfactant chosen from polysorbate20, polysorbate 80, and mixtures thereof; wherein the at least onesurfactant comprises less than 35%, by weight relative the weight of thepreconcentrate.

In some embodiments, for example, the pharmaceutical preconcentratecomprises K85EE as the fatty acid oil mixture, and at least onesurfactant chosen from polysorbate 20, polysorbate 80, and mixturesthereof.

In another embodiment, the pharmaceutical preconcentrate comprises afatty acid oil mixture comprising from about 80% to about 88% EPA andDHA, by weight of the fatty acid oil mixture, wherein the EPA and DHAare in ethyl ester form; at least one surfactant chosen from polysorbate80; and at least one co-surfactant comprising ethanol.

In some embodiments, the pre-concentrate is in the form of a gelatincapsule or loaded into a tablet.

In other embodiments, the preconcentrate is a food supplementpreconcentrate or nutritional supplement preconcentrate comprising afatty acid oil mixture comprising from about 25% to about 75% EPA andDHA, by weight of the fatty acid oil mixture, wherein the EPA and DHAare in a form chosen from ethyl ester and triglyceride; and at least onesurfactant.

In some embodiments, the weight ratio of fatty acid oil mixture:totalsurfactant of the preconcentrate ranges from about 1:1 to about 200:1,from about 1:1 to about 100:1, from about 1:1 to about 50:1, from about1:1 to about 10:1, from about 1:1 to about 8:1, from about 1.1 to 6:1from about 1:1 to about 5:1, from about 1:1 to about 4:1, or from about1:1 to about 3:1.

In some embodiments, the at least one surfactant comprises from about0.5% to about 40%, by weight relative to the total weight of thepreconcentrate. For example, in some embodiments, the at least onesurfactant comprises from about 1% to about 35%, from about 5% to about35%, from about 10% to about 35%, from about 15% to about 35%, fromabout 15% to about 30%, or from about 20% to about 30%, by weight,relative to the total weight of the preconcentrate. In one embodiment,the at least one surfactant comprises about 20%, by weight relative tothe total weight of the preconcentrate.

SNEDDS/SMEDDS/SEDDS

The preconcentrate of the present disclosure may be in a form of aself-nanoemulsifying drug delivery system (SNEDDS), aself-microemulsifying drug delivery system (SMEDDS), or a selfemulsifying drug delivery system (SEDDS), wherein the preconcentrateforms an emulsion in an aqueous solution.

Without being bound by theory, it is believed that the preconcentrateforms a SNEDDS, SMEDDS, and/or SEDDS upon contact with gastric and/orintestinal media in the body, wherein the preconcentrate forms anemulsion comprising micelle particles. The emulsion may, for example,provide for increased or improved stability of the fatty acids foruptake in the body and/or provide increased surface area for absorption.SNEDDS/SMEDDS/SEDDS may thus provide for enhanced or improvedhydrolysis, solubility, bioavailability, absorption, or any combinationsthereof of fatty acids in vivo.

Generally, known SNEDDS/SMEDDS/SEDDS formulations comprise ˜10 mg of adrug and ˜500 mg of surfactants/co-surfactants. The SNEDDS/SMEDDS/SEDDSpresently disclosed may have the opposite relationship, i.e., the amountof fatty acid oil mixture comprising the active pharmaceuticalingredient (API) is greater than the amount of surfactant.

The SNEDDS/SMEDDS/SEDDS presently disclosed may comprise a particle size(i.e., particle diameter) ranging from about 5 nm to about 10 μm. Forexample, in some embodiments, the particle size ranges from about 5 nmto about 1 μm, such as from about 50 nm to about 750 nm, from about 100nm to about 500 nm, or from about 150 nm to about 350 nm.

Excipients

The compositions presently disclosed may further comprise at least onenon-active pharmaceutical ingredient, e.g., excipient. Non-activeingredients may solubilize, suspend, thicken, dilute, emulsify,stabilize, preserve, protect, color, flavor, and/or fashion activeingredients into an applicable and efficacious preparation, such that itmay be safe, convenient, and/or otherwise acceptable for use. The atleast one non-active ingredient may be chosen from colloidal silicondioxide, crospovidone, lactose monohydrate, lecithin, microcrystallinecellulose, polyvinyl alcohol, povidone, sodium lauryl sulfate, sodiumstearyl fumarate, talc, titanium dioxide, and xanthum gum.

The compositions presently disclosed may further comprise at least oneantioxidant. Examples of antioxidants suitable for the presentdisclosure include, but are not limited to, α-tocopherol (vitamin E),calcium disodium EDTA, alpha tocoferyl acetates, butylhydroxytoluenes(BHT), and butylhydroxyanisoles (BHA).

The compositions presently disclosed may further comprise at least onesuperdistintegrant. Superdisintegrants may, for example, improvedisintegrant efficiency resulting in decreased use levels in comparisonto traditional disintegrants. Examples of superdisintegrants include,but are not limited to, crosscarmelose (a crosslinked cellulose),crospovidone (a crosslinked polymer), sodium starch glycolate (acrosslinked starch), and soy polysaccharides. Commercial examples ofsuperdisintegrants include Kollidon® (BASF), Polyplasdone® XL (ISP), andAc-Di-Sol (FMC BioPolymer).

In some embodiments of the present disclosure, the composition comprisesfrom about 1% to about 25% of at least one superdisintegrant by weightof the composition, such as from about 1% to about 20% by weight, orfrom about 1% to about 15% by weight of the composition. In someembodiments, the compositions comprising at least one superdisintegrantare in a tablet form.

The compositions presently disclosed may be administered, e.g., incapsule, tablet or any other drug delivery forms. For example, thecomposition may be encapsulated, such as in a gelatin capsule. In someembodiments, the preconcentrate is encapsulated in a gelatin capsule.

In some embodiments of the present disclosure, the capsule fill contentranges from about 0.400 g to about 1.600 g. For example, in someembodiments, the capsule fill content ranges from about 0.400 g to about1.300 g, from about 0.600 g to about 1.200 g, from about 0.600 g toabout 0.800 g, from about 0.800 g to about 1.000, from about 1.000 g toabout 1.200 g, or any amount in between. For example, in someembodiments the capsule fill content is about 0.600 g, about 0.800 g,about 1.000 g, or about 1.200 g.

The capsules presently disclosed may be manufactured in low oxygenconditions to inhibit oxidation during the manufacturing process.Preparation of capsules and/or microcapsules in accordance with thepresent disclosure may be carried out following any of the methodsdescribed in the literature. Examples of such methods include, but arenot limited to, simple coacervation methods (see, e.g., ES 2009346, EP0052510, and EP 0346879), complex coacervation methods (see, e.g., GB1393805), double emulsion methods (see, e.g., U.S. Pat. No. 4,652,441),simple emulsion methods (see, e.g., U.S. Pat. No. 5,445,832), andsolvent evaporation methods (see, e.g., GB 2209937). Those methods may,for example, provide for continuous processing and flexibility of batchsize.

Methods or Uses

The present disclosure further encompasses methods of treating and/orregulating at least one health problem in a subject in need thereof. Thecompositions presently disclosed may be administered, e.g., in capsule,tablet or any other drug delivery forms, to a subject for therapeutictreatment and/or regulation of at least one health problem including,for example, irregular plasma lipid levels, cardiovascular functions,immune functions, visual functions, insulin action, neuronaldevelopment, heart failure, and post myocardial infarction. In someembodiments, the at least one health problem is chosen from mixeddyslipidemia, dyslipidemia, hypertriglyceridemia, hypercholesterolemia,heart failure, and post-myocardial infarction.

In one embodiment, there is a method of treating at least one healthproblem in a subject in need thereof, comprising administering to thesubject a pharmaceutical preconcentrate comprising apharmaceutically-effective amount of a fatty acid oil mixture comprisingat least 75% eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA),by weight of the fatty acid oil mixture, wherein the EPA and DHA are ina form chosen from ethyl ester and triglyceride; and at least onesurfactant. In some embodiments, the method treats at least one ofelevated triglyceride levels, non-HDL cholesterol levels, LDLcholesterol levels and/or VLDL cholesterol levels.

In another embodiment, there is a method of regulating at least onehealth problem in a subject in need thereof, comprising administering tothe subject administering to the subject a supplement preconcentratecomprising: a fatty acid oil mixture comprising from about 25% to about75% eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), byweight of the fatty acid oil mixture, wherein the EPA and DHA are in aform chosen from ethyl ester and triglyceride; and at least onesurfactant; wherein the at least one health problem is chosen fromirregular plasma lipid levels, cardiovascular functions, immunefunctions, visual functions, insulin action, neuronal development, heartfailure, and post myocardial infarction.

In some embodiments, the pharmaceutical or supplement preconcentrateforms a self-nanoemulsifying drug delivery system (SNEDDS), aself-microemulsifying drug delivery system (SMEDDS), or aself-emulsifying drug delivery system (SEDDS) in an aqueous solution. Insome embodiments, the aqueous solution is gastric media and/orintestinal media.

The total daily dosage of the fatty acid oil mixture may range fromabout 0.600 g to about 6.000 g. For example, in some embodiments, thetotal dosage of the fatty acid oil mixture ranges from about 0.800 g toabout 4.000 g, from about 1.000 g to about 4.000 g, or from about 1.000g to about 2.000 g. In one embodiment, the fatty acid oil mixture ischosen from K85EE and AGP 103 fatty acid oil compositions.

The preconcentrates presently disclosed may be administered in from 1 to10 dosages, such as from 1 to 4 times a day, such as once, twice, threetimes, or four times per day, and further for example, once, twice orthree times per day. The administration may be oral or any other form ofadministration that provides a dosage of fatty acids, e.g., omega-3fatty acids, to a subject.

The following examples are intended to illustrate the present disclosurewithout, however, being limiting in nature. It is understood that theskilled artisan will envision additional embodiments consistent with thedisclosure provided herein.

EXAMPLES Example 1 Compatibility of Preconcentrates with Solvents

The compatibility of solvents and a preconcentrate having a fixed amountof K85EE and Tween-80 were evaluated. The preconcentrates described inTable 8 were prepared according to the schemes below on a weight toweight basis. The preconcentrates were visually inspected after mixingand again after being stored for 24 hours at room temperature. Under thePreconcentrate heading, a “clear” designation represents a transparenthomogenous mixture; a “turbid” designation represents a nonhomogenousmixture, where some turbidity can be observed by visual inspection. Thedegree of turbidity was not determined.

TABLE 8 Compatibility of Solvent and Preconcentrates. K85-EE Tween-8096% ethanol 96% ethanol Preconcen- (mg) (mg) (mg) (%) trate 400 110 10.72.1 Turbid 400 110 18.7 3.5 Turbid 400 110 28.4 5.3 Turbid 400 110 32.15.9 Turbid 400 110 45.7 8.2 Turbid 400 110 53.5 9.5 Turbid 400 110 61.510.8 Turbid 400 110 69.8 12.0 Turbid 400 110 79.9 13.5 Turbid 400 11091.3 15.2 Turbid 400 110 102.5 16.7 Turbid Propylene Propylene K85-EETween-80 glycol glycol Preconcen- (mg) (mg) (mg) (%) trate 400 110 11.12.1 Turbid 400 110 16.7 3.2 Turbid 400 110 23.1 4.3 Turbid 400 110 32.96.1 Turbid 400 110 41.5 7.5 Turbid 400 110 48.6 8.7 Turbid 400 110 59.910.5 Turbid 400 110 72.9 12.5 Turbid 400 110 81.5 13.8 Turbid 400 11093.5 15.5 Turbid 400 110 104.6 17.0 Turbid K85-EE Tween-80 PEG 300 PEG300 Preconcen- (mg) (mg) (mg) (%) trate 400 110 13.9 2.7 Turbid 400 11023.7 4.4 Turbid 400 110 35.6 6.5 Turbid 400 110 47.1 8.5 Turbid 400 11055.0 9.7 Turbid 400 110 68.7 11.9 Turbid 400 110 81.8 13.8 Turbid 400110 90.3 15.0 Turbid 400 110 104.0 16.9 Turbid Benzyl Benzyl K85-EETween-80 alcohol alcohol Preconcen- (mg) (mg) (mg) (%) trate 400 110 0 0Clear 400 110 11.4 2.2 Turbid 400 110 18.1 3.4 Turbid 400 110 30.9 5.7Clear 400 110 45.5 8.2 Clear 400 110 55.6 9.8 Clear 400 110 66.7 11.6Clear 400 110 77.4 13.2 Clear 400 110 92.1 15.3 Clear 400 110 99.0 16.3Clear K85-EE Tween-80 Triacetin Triacetin Preconcen- (mg) (mg) (mg) (%)trate 400 110 12.3 2.4 Turbid 400 110 24.3 4.5 Turbid 400 110 35.8 6.6Turbid 400 110 45.3 8.2 Turbid 400 110 57.0 10.1 Turbid 400 110 68.111.8 Turbid 400 110 80.9 13.7 Turbid 400 110 90.0 15.0 Turbid 400 110101.7 16.6 Turbid 1-octa- 1-octa- K85-EE Tween-80 decanol 99% decanol99% Preconcen- (mg) (mg) (mg) (%) trate 400 110 8.6 1.7 Precipitateoleyl oleyl K85-EE Tween-80 alcohol 85% alcohol 85% Preconcen- (mg) (mg)(mg) (%) trate 400 100 13.0 2.5 Turbid 400 100 26.5 4.9 Turbid 400 10037.3 6.8 Turbid 400 100 49.5 8.8 Turbid 400 100 62.6 10.9 Turbid 400 10077.7 13.2 Turbid 400 100 92.2 15.3 Turbid 400 100 105.7 17.2 Turbid1-tetra- 1 tetra- K85-EE Tween-80 decanol 97% decanol 97% Preconcen-(mg) (mg) (mg) (%) trate 400 100 1.7 0.3 Turbid 400 100 10.3 2.0 Turbid400 100 22.7 4.3 Turbid 400 100 35.8 6.6 Precipitate K85-EE Tween-80glycerol glycerol Preconcen- (mg) (mg) (mg) (%) trate 400 100 17.7 3.4Turbid 400 100 28.0 5.2 Turbid 400 100 41.7 7.6 Turbid 400 100 52.8 9.4Turbid 400 100 71.2 12.3 Turbid 400 100 85.4 14.3 Turbid 400 100 92.315.3 Turbid 400 100 105.7 17.2 Turbid Oleic Oleic K85-EE Tween-80 acid90% acid 90% Preconcen- (mg) (mg) (mg) (%) trate 400 100 13.2 2.5 Turbid400 100 23.9 4.5 Turbid 400 100 31.5 5.8 Turbid 400 100 41.4 7.5 Turbid400 100 51.8 9.2 Turbid 400 100 65.2 11.3 Clear 400 100 79.8 13.5 Clear400 100 87.2 14.6 Clear 400 100 102.2 16.7 Clear 1-docosanol 1-docosanolK85-EE Tween-80 98% 98% Preconcen- (mg) (mg) (mg) (%) trate 400 100 9.61.8 Precipitate

Example 2 Lipolysis and Solubilization

Studies were done to analyze the rate of lipolysis (i.e., hydrolysis)and solubilization for different preconcentrates comprising K85EE anddifferent free fatty acids and surfactants. Specifically, fourexperiments were designed to determine how the amount of surfactantinfluences the rate and extent of lipolysis and solubilization. Thelipolysis was conducted on SMEDDS formulations comprising K85EE.

Materials

-   -   Bile salts: Porcine Bile extract (Sigma); contains glycine and        taurine conjugates of hyodeoxycholic acid and other bile salts.    -   Pancreatic lipase, Porcine pancreas (Sigma); contains many        enzymes, including amylase, trypsin, lipase, ribonuclease and        protease.    -   Lechitin: Phospholipids (LIPOID S PC from LIPOID AG)    -   Trizma maleate (Sigma Aldrich)    -   Tween 20, Molecular Biology Grade (AppliChem Darmstadt), Tween        80 (Fluka)    -   α-Linoleic acid (Sigma 60%), Oleic acid (Aldrich 90%)    -   K85-EE and K85-FA

Preconcentrates A-E were prepared as summarized in Table 9.

TABLE 9 Preconcentrates A-E. Preconcen- Fatty acid trate oil mixtureFree fatty acid Surfactant A K85EE (400 mg) oleic acid Tween 20 (300 mg)(100 mg) B K85EE (400 mg) oleic acid Tween 20 (75 mg) (100 mg) C K85EE(500 mg) linoleic acid Tween 80 (200 mg) (100 mg) D K85EE (400 mg) K85FA(100 mg) Tween 20 (300 mg) E K85EE (400 mg) — Tween 80 (100 mg)

Lipolysis General Procedure

The in vitro dynamic lipolysis model developed by Zangenberg et al.(Zangenberg, N. H. et al., Eur. J. Pharm. Sci. 14, 237-244, 2001;Zangenberg, N. H., et al., Eur. J. Pharm. Sci. 14, 115-122, 2001) wasused with slight modifications. The lipolysis was conducted in athermostated 600 ml jacketed glass vessel in the presence of porcinebile extract, with continuous addition calcium chloride. The lipasesource was porcine pancreatin and the hydrolysis was followed bytitration with sodium hydroxide solution (1.0 N) using a pH stat (pH6.5). The initial composition of the lipolysis media is shown in Table10.

TABLE 10 Initial composition of lipolysis media. Substance Initialconcentration Pancreatic lipase, Porcine pancreas 800 USP units/ml Bilesalts, Porcine Bile extract 5 mM Phospholipids, LIPOID S PC from LIPOIDAG 1.25 mM Trizma maleate 2 mM Na⁺ 150 mM K85-EE 5.58 mg/ml

The final volume in all experiments was 300 ml and the calciumdispensing rate during the experiments was 0.045 mmol/min (0.09 ml/min).In all experiments, the amount of K85-EE added corresponds to 5.58mg/ml.

To determine the course of K85-EE lipolysis by HPLC, crude samples werewithdrawn and acidified with dilute hydrochloric acid. Theconcentrations of EPA-EE, DHA-EE, EPA-FA and DHA-FA were determined byHPLC in triplicate. Experiments were performed with LC AgilentTechnologies 1200 series at a column temperature of 30° C., mobile phase(A) water (0.1% acetic acid) and (B) MeCN (0.1% acetic acid), withgradient: 0 to 8 minutes, from 70% B to 100% B; 8 to 15 minutes, 100% B;16 to 16 minutes: from 100% B to 70% B, 16 to 20 minutes: 70% B. Theflow rate was 0.5 ml/min, UV @ 210 nM, injection volume: 5 μl, and runtime: 20 minutes.

Concentrations of EPA ethyl ester (EPA-EE), DHA ethyl ester (DHA-EE),EPA free acid (EPA-FA), and DHA free acid (DHA-FA) were monitored overtime and the rate of lipolysis calculated as shown in Table 11 forcomparison with Omacor®.

TABLE 11 Lipolysis of EPA and DHA ethyl ester in comparison to Omacor ®.% lipolysis EPA-EE lipolysis DHA-EE lipolysis K85EE at (μg/ml/min)(μg/ml/min) t = 233 min Omacor 1.5 2.3 17 A 2.8 4.5 41 B 2.9 3.9 35 C3.7 5.0 47 D 3.5 5.0 55 E 3.8 4.3 45

FIGS. 1, 4, 7, 10, 3, and 16 graphically illustrate the disappearance ofEPA-EE and DHA-EE and the appearance of EPA-FA and DHA-FA duringlipolysis of each respective sample examined. Sample points from 2minutes to 233 minutes were included in the graphs. In addition, linearregression lines have been included.

FIGS. 2, 5, 8, 11, 14, and 17 provide the percent recover of EPA+DHA atdifferent time-points for each respective sample examined. Data aregiven as the sum of EPA-EE, DHA-EE, EPA-FA, and DHA-FA and given as apercentage of theoretical amount 5580 μg/ml.

FIGS. 3, 6, 9, 12, 15, and 18 graphically illustrate the percentlipolysis at different time points for EPA-EE, DHA-EE and total K85EE.Values are calculated relative to the total amount of EPA-EE and DHA-EEdetermined by HPLC after lipolysis for 2 minutes.

Example 3 Emulsions in Pure Water

The oil content in one capsule OMACOR®, comprising EPA ethyl ester (465mg), DHA ethyl ester (375 mg) and alpha-tochopherol (4 mg) were mixed ina scintillation vial with various surfactants as shown below in Table12. Water (10 ml) was added at 37 degrees centigrade and the mixture wasshaken for 15 seconds using a Vortex mixer. The mixture was observedafter 1 minute and after 5 minutes. The visual score for emulsionhomogeneity was scored as follows: No emulsion=score 0, emulsion but nothomogeneous emulsion=score 1, homogenous emulsion=score 2.

The mixture was after mixing also rolled in a roller mixer for 5minutes. The visual score for this roller test was the same as above.

TABLE 12 Emulsions in pure water. Score After Score Refer- Amount ofVortex After Score ence Surfactant for 1 Vortex 5 Roller No.Surfactant(s) (mg) minute minutes Mixer 1 None 0 0 0 0 2 Brij ® 30 100 22 2 3 Brij ® 35 100 2 1 2 4 Brij ® 52 100 2 2 2 5 Brij ® 58 100 2 1 2 6Brij ® 72 100 2 1 2 7 Brij ® 78 100 2 1 2 8 Brij ® 92V 100 2 2 2 9Brij ® 93 100 2 2 2 10 Brij ® 96V 100 2 2 2 11 Brij ® 97 100 2 2 2 12Brij ® 98 100 2 1 2 13 Brij ® 700 100 1 1 2 14 Brij ® S-10 100 1 1 2 15Pluronic ® L-31 100 1 1 2 16 Pluronic ® L-35 100 1 1 2 17 Pluronic ®L-81 100 2 2 2 18 Pluronic ® L-64 100 2 2 2 19 Pluronic ® L-121 100 2 22 20 Pluronic ® P-123 100 1 1 2 21 Pluronic ® F-68 100 0 0 1 22Pluronic ® F-108 100 0 0 1 23 Span ® 20 100 2 2 2 24 Span ® 60 100 0 0 125 Span ® 65 100 0 0 0 26 Span ® 80 100 1 1 2 27 Span ® 85 100 0 0 1 28Tween ® 20 100 2 1 2 29 Tween ® 40 100 2 1 2 30 Tween ® 60 100 2 1 2 31Tween ® 80 100 2 1 2 32 Alginic Acid 100 1 0 1 33 Alginic Acid 100 2 1 1sodium salt 34 Macrogolglycerol- 100 2 2 2 hydroxystearas 40 35 Sodiumlauryl 100 1 1 2 sulphate 36 1,2-Dipalmitoyl-sn- 100 0 0 0 glycerolethanolamine 37 1-Hexadecanol 100 1 0 0 38 1,2-Dipalmitoy-sn 100 2 1 139 Macrogol 400 100 0 0 1 40 Myristic acid 100 1 1 1 sodium salt 41Brij ® 52/ 30/20 2 2 2 Macrogolglycerol- hydroxystearas 40 42 Brij ® 62/30/50 2 2 2 Pluronic ® L64 43 Span ® 20/ 40/90 2 2 2 Pluronic ® L64 44Macrogol 400/ 120/60  2 2 2 Macrogol-glycerol- hydroxystearas 40 45Tween ® 20/ 60/60 2 2 2 Span ® 20 46 Tween ® 20/ 90/90/60 2 2 2 Span ®20/ Macrogol 400 47 Span ® 20/ 70/100/40 2 2 2 Tween ® 20/ Brij ® 97 48Alginic acid sodium 110/60  2 2 2 salt/Span ® 60 49 Pluronic ® F-68/20/180/20 2 2 2 Pluronic ® L64/ Span ® 60

Example 4 Emulsions in Artificial Gastric Juice

The oil content in one capsule OMACOR®, comprising EPA ethyl ester (465mg), DHA ethyl ester (375 mg) and alpha-tochopherol (4 mg) were mixed ina scintillation vial with various surfactants as shown below in Table13. The experimental set up in the examples below is the same asdescribed previously except that that artificial gastric juice withoutpepsin (European Pharmacopeia 6.0, page 274) was used instead of water.

TABLE 13 Emulsions in artificial gastric juice Score Score After afterRefer- Amount of Vortex Vortex Score ence Surfactant for 1 for 5 RollerNo. Surfactant(s) (mg) minute minutes Mixer 50 None 0 0 0 0 51 Brij ® 52100 2 1 2 52 Brij ® 96V 100 2 1 2 53 Pluronic ® L64 100 2 2 2 54 Tween ®40 100 2 2 2 55 Macrogolglycerol- 100 2 2 2 Hydroxysteraras 40

Example 5 Emulsions in Simulated Intestinal Fluid

The oil content in one capsule OMACOR®, comprising EPA ethyl ester (465mg), DHA ethyl ester (375 mg) and alpha-tochopherol (4 mg) were mixed ina scintillation vial with various surfactants as shown below in Table14. The experimental set up in the examples below is the same asdescribed previously except that that simulated intestinal fluid pH 6.8without pancreas powder (European Pharmacopeia 6.0, page 274) was usedinstead of water.

TABLE 14 Emulsions in simulated intestinal fluid. Score Score Afterafter Refer- Amount of Vortex Vortex Score ence Surfactant for 1 for 5Roller No. Surfactant(s) (mg) minute minutes Mixer 56 None 0 0 0 0 57Brij ® 52 100 2 2 2 58 Brij ® 96V 100 2 2 2 59 Pluronic ® L64 100 2 2 260 Tween ® 40 100 2 2 2 61 Macrogolglycerol- 100 2 2 2 Hydroxysteraras40

Example 6 Microscopic Examination of Emulsions

Emulsions from Example 52 (gastric juice) and Example 58 (intestinalfluid) were examined under the microscope after 24 hours rolling. Bothemulsions were found to be suspensions of oil in water with no tendencyto aggregation.

Example 7 Pharmaceutical Formulations

The following examples in Table 15 illustrate pharmaceuticalformulations that can be prepared.

TABLE 15 Pharmaceutical Formulations K85EE or Example AGP103 Oil No.Mixture Surfactant or Surfactant System 64 X Tween ® 20 65 X Tween ® 4066 X Tween ® 80 67 X Tween ® 20 + Tween ® 40 68 X Tween ® + Cremphor ®69 X Tween ® + Solutol HS 15

In an embodiment, the surfactant or combination of surfactants is chosenfrom Tween® surfactants; Tween® 20, Tween® 40, Tween® 60, Tween® 65,Tween® 80 and Tween® 85.

In another embodiment, the surfactant is chosen from a combination of aTween® surfactants and a surfactant chosen from Cremphor®, for instanceTween® 20 and Cremphor EL. Moreover, in a further embodiment, a Tween®20 and Solutol HS 15 surfactant can be used together as well as Tween®20 and Tween® 40.

Fatty acid oil mixtures of pharmaceutical preconcentrates, wherein thefatty acid oil mixture is a K85EE or AGP-103 oil composition arepresented in Table 16.

TABLE 16 Fatty acid oil mixture for pharmaceutical preconcentrates.Fatty acid oil mixture: 1000 mg K85EE fatty acid oil mixture MinimumValue Maximum Value EPAEE + DHAEE 800 mg/g 880 mg/g EPAEE 430 mg/g 495mg/g DHAEE 347 mg/g 403 mg/g Total omega-3 EE >90% (w/w) EE = ethylester

Example 8 Additional Emulsions in Artificial Gastric Juice and SimulatedIntestinal Fluid

Preconcentrates 1-23 were prepared with EPA/DHA ethyl ester (1000 mgK85EE) and various surfactants and surfactant mixtures as shown in Table17 below. Emulsions were prepared in both gastric juice and simulatedintestinal fluid as described in Examples 4 and 5. Results were the samefor emulsions in artificial gastric juice and simulated intestinalfluid, and appear in Table 17.

TABLE 17 Emulsions in artificial gastric juice and simulated intestinalfluid. Score After Score Refer- Amount of Vortex After Score enceSurfactant for 1 Vortex 5 Roller No. Surfactant(s) (mg) minute minutesMixer 1 Cremophor ® EL 20 2 1 2 2 Cremophor ® EL 80 2 1 2 3 Cremophor ®EL 100 2 1 2 4 Cremophor ® EL 150 2 2 2 5 Cremophor ® EL 200 2 2 2 6Cremophor ® EL 250 2 2 2 7 Cremophor ® EL 300 2 2 2 8 Cremophor ® EL 4002 2 2 9 Cremophor ® EL 500 2 2 2 10 Cremophor ® EL 600 2 2 2 11Cremophor ® EL 700 2 2 2 12 Cremophor ® EL 800 2 2 2 13 Cremophor ® EL900 2 2 2 14 Cremophor ® EL 1000 2 2 2 15 Cremophor ® EL 1200 2 2 2 16Cremophor ® EL 150 2 2 1 Tween ® 60 100 17 Cremophor ® EL 40 2 2 2Brij ® 30 20 Span ® 85 20 18 Cremophor ® EL 5 2 1 2 19 Cremophor ® EL 602 1 2 Tween ® 80 70 20 Macrogolglyceroli 60 2 1 2 Hydroxystearas 40 21Macrogolglyceroli 90 2 1 2 Hydroxystearas 40 Span ® 20 30 Polysorbate 2050 22 Macrogolglyceroli 60 2 1 2 Hydroxystearas 40 Brij ® 93 30Polysorbate 20 60 23 Cremophor ® EL 60 2 2 2 Pluronic ® F68 30 Brij ®92V 30 Polysorbate 20 20

Emulsions 4-15 prepared in both artificial gastric juice and simulatedintestinal fluid were homogenous (milky) for several hours whenstanding. Emulsions 1-3 separated somewhat after preparation (i.e.,after several hours of standing). Microscopy of Emulsions 1-15 showedthat the average particle size was less than 100 micrometers.Homogenization treatment (UltraRurrax(IKA)) of Emulsion 4 for 20 secondsresulted in a substantial increase of formation of small particles (<10microns).

Based on the preconcentrates prepared, a 0.5% non-ionic surfactant(e.g., Cremophor®) can emulsify EPA/DHA ethyl ester in both artificialgastric juice and simulated intestinal fluid. In addition, includingmore than one surfactant appears to stabilize the emulsion. Further, theparticle size can vary depending upon the emulsification method.

What is claimed is:
 1. A preconcentrate comprising: a fatty acid oilmixture comprising at least 75% eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA), by weight of the fatty acid oil mixture,wherein the EPA and DHA are in a form chosen from ethyl ester andtriglyceride; and from about 0.5% to about 40% of at least one nonionicsurfactant chosen from polysorbate 20, polysorbate 80, and mixturesthereof, by weight relative to the total weight of the preconcentrate,wherein the at least one nonionic surfactant enhances lipolysis of EPAand DHA ethyl esters; and wherein the preconcentrate does not comprise apharmaceutically active agent other than the fatty acid oil mixture. 2.The preconcentrate according to claim 1, wherein of the at least 75% EPAand DHA of the fatty acid oil mixture, at least 95% is EPA.
 3. Thepreconcentrate according to claim 1, wherein of the at least 75% EPA andDHA of the fatty acid oil mixture, at least 95% is DHA.
 4. Thepreconcentrate according to claim 1, wherein the fatty acid oil mixturecomprises at least 90% omega-3 fatty acids, by weight of the fatty acidoil mixture.
 5. The preconcentrate according to claim 4, wherein atleast one of the omega-3 fatty acids has a cis configuration.
 6. Thepreconcentrate according to claim 1, wherein the fatty acid oil mixturefurther comprises at least one other fatty acid other than EPA and DHAchosen from α-linolenic acid (ALA), heneicosapentaenoic acid (HPA),docosapentaenoic acid (DPA), eicosatetraenoic acid (ETA), eicosatrienoicacid (ETE), stearidonic acid (STA), linoleic acid, gamma-linolenic acid(GLA), arachidonic acid (AA), osbond acid, and mixtures thereof.
 7. Thepreconcentrate according to claim 1, wherein the fatty acid oil mixtureis derived from at least one oil chosen from marine oil, algae oil,plant-based oil, and microbial oil.
 8. The preconcentrate according toclaim 7, wherein the marine oil is a purified fish oil.
 9. Thepreconcentrate according to claim 1, wherein the EPA:DHA weight ratio ofthe fatty acid oil mixture ranges from about 1:10 to 10:1.
 10. Thepreconcentrate according to claim 1, wherein the preconcentratecomprises from about 10% to about 30% of the at least one nonionicsurfactant, by weight relative to the total weight of thepreconcentrate.
 11. The preconcentrate according to claim 10, whereinthe preconcentrate comprises about 20% of the at least one nonionicsurfactant, by weight relative to the total weight of thepreconcentrate.
 12. The preconcentrate according to claim 1, furthercomprising at least one co-surfactant chosen from short chain alcohols,glycol ethers, pyrrolidine derivatives, 2-pyrrolidone, bile salts, andmixtures thereof.
 13. The preconcentrate according to claim 12, whereinthe preconcentrate comprises from about 1% to about 10% of the at leastone co-surfactant, by weight relative to the total weight of thepreconcentrate.
 14. The preconcentrate according to claim 1, wherein theweight ratio of fatty acid oil mixture:total surfactant ranges fromabout 1:1 to about 200:1.
 15. The preconcentrate according to claim 1,wherein the preconcentrate further comprises at least onepharmaceutically-acceptable solvent chosen from lower alcohols andpolyols.
 16. The preconcentrate according to claim 1, further comprisingat least one antioxidant in an amount less than apharmaceutically-effective amount.
 17. The preconcentrate according toclaim 16, wherein the at least one antioxidant is chosen frombutylhydroxyanisoles (BHA) and α-tocopherol.
 18. The preconcentrateaccording to claim 1, wherein the fatty acid oil mixture is present in apharmaceutically-effective amount.
 19. The preconcentrate according toclaim 1, wherein the preconcentrate is in the form of a gelatin capsule.20. The preconcentrate according to claim 19, wherein the capsule fillcontent ranges from about 0.400 g to about 1.300 g.
 21. Thepreconcentrate according to claim 1, wherein the fatty acid oil mixturecomprises from about 80% to about 88% EPA and DHA, by weight of thefatty acid oil mixture, wherein the EPA and DHA are in ethyl ester form.22. The preconcentrate according to claim 21, further comprising atleast one co-surfactant comprising ethanol.
 23. A self-nanoemulsifyingdrug delivery system (SNEDDS), self-microemulsifying drug deliverysystem (SMEDDS), or self-emulsifying drug delivery system (SEDDS)comprising a preconcentrate comprising: a fatty acid oil mixturecomprising from about 80% to about 88% eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA), by weight of the fatty acid oil mixture,wherein the EPA and DHA are in a form chosen from ethyl ester andtriglyceride; and from about 0.5% to about 40% of at least one nonionicsurfactant chosen from polysorbate 20, polysorbate 80, and mixturesthereof, by weight relative to the total weight of the preconcentrate,wherein the at least one nonionic surfactant enhances lipolysis of EPAand DHA ethyl esters; wherein the preconcentrate forms an emulsion in anaqueous solution; and wherein the preconcentrate does not comprise apharmaceutically active agent other than the fatty acid oil mixture. 24.The system according to claim 23, wherein the fatty acid oil mixturecomprises at least 90% omega-3 fatty acids, by weight of the fatty acidoil mixture.
 25. The system according to claim 24, wherein at least oneof the omega-3 fatty acids has a cis configuration.
 26. The systemaccording to claim 23, wherein the fatty acid oil mixture furthercomprises at least one other fatty acid other than EPA and DHA chosenfrom α-linolenic acid (ALA), heneicosapentaenoic acid (HPA),docosapentaenoic acid (DPA), eicosatetraenoic acid (ETA), eicosatrienoicacid (ETE), stearidonic acid (STA), linoleic acid, gamma-linolenic acid(GLA), arachidonic acid (AA), osbond acid, and mixtures thereof.
 27. Thesystem according to claim 23, wherein the fatty acid oil mixture isderived from at least one oil chosen from marine oil, algae oil,plant-based oil, and microbial oil.
 28. The system according to claim27, wherein the marine oil is a purified fish oil.
 29. The systemaccording to claim 23, wherein the EPA:DHA weight ratio of the fattyacid oil mixture ranges from about 1:10 to 10:1.
 30. The systemaccording to claim 23, wherein the preconcentrate comprises from about10% to about 30% of the at least one nonionic surfactant, by weightrelative to the total weight of the preconcentrate.
 31. The systemaccording to claim 30, wherein the preconcentrate comprises about 20% ofthe at least one nonionic surfactant, by weight relative to the totalweight of the preconcentrate.
 32. The system according to claim 23,wherein the preconcentrate further comprises at least one co-surfactantchosen from short chain alcohols, glycol ethers, pyrrolidinederivatives, 2-pyrrolidone, bile salts, and mixtures thereof.
 33. Thesystem according to claim 32, wherein the preconcentrate comprises fromabout 1% to about 10% of the at least one co-surfactant, by weightrelative to the total weight of the preconcentrate.
 34. The systemaccording to claim 23, wherein the weight ratio of fatty acid oilmixture:total surfactant ranges from about 1:1 to about 200:1.
 35. Thesystem according to claim 23, wherein the preconcentrate furthercomprises at least one pharmaceutically-acceptable solvent chosen fromlower alcohols and polyols.
 36. The system according to claim 23,wherein the preconcentrate further comprises at least one antioxidant inan amount less than a pharmaceutically-effective amount.
 37. The systemaccording to claim 36, wherein the at least one antioxidant is chosenfrom butylhydroxyanisoles (BHA) and α-tocopherol.
 38. The systemaccording to claim 23, wherein the fatty acid oil mixture is present ina pharmaceutically-effective amount.
 39. The system according to claim23, wherein the system is in the form of a gelatin capsule.
 40. Thesystem according to claim 39, wherein the capsule fill content rangesfrom about 0.400 g to about 1.300 g.
 41. The system according to claim23, wherein the particle size of the emulsion ranges from about 150 nmto about 350 nm.
 42. A method of treating at least one health problem ina subject in need thereof comprising administering to the subject apharmaceutical preconcentrate comprising: a fatty acid oil mixturecomprising at least 75% eicosapentaenoic acid (EPA) and docosahexaenoicacid (DHA), by weight of the fatty acid oil mixture, wherein the EPA andDHA are in a form chosen from ethyl ester and triglyceride; and at leastone nonionic surfactant chosen from polysorbate 20, polysorbate 80, andmixtures thereof; wherein the pharmaceutical preconcentrate does notcomprise a pharmaceutically active agent other than the fatty acid oilmixture; and wherein the at least one health problem is chosen fromcardiovascular functions, immune functions, visual functions, insulinaction, neuronal development, heart failure, post myocardial infarction,mixed dyslipidemia, dyslipidemia, hypertriglyceridemia, andhypercholesterolemia.
 43. The method according to claim 42, wherein theat least one health problem is chosen from elevated triglyceride levels,non-HDL cholesterol levels, LDL cholesterol levels and/or VLDLcholesterol levels.
 44. The method according to claim 42, wherein thefatty acid oil mixture comprises at least 90% omega-3 fatty acids, byweight of the fatty acid oil mixture.
 45. The method according to claim44, wherein at least one of the omega-3 fatty acids has a cisconfiguration.
 46. The method according to claim 42, wherein the fattyacid oil mixture further comprises at least one other fatty acid otherthan EPA and DHA chosen from α-linolenic acid (ALA), heneicosapentaenoicacid (HPA), docosapentaenoic acid (DPA), eicosatetraenoic acid (ETA),eicosatrienoic acid (ETE), stearidonic acid (STA), linoleic acid,gamma-linolenic acid (GLA), arachidonic acid (AA), osbond acid, andmixtures thereof.
 47. The method according to claim 42, wherein thefatty acid oil mixture is derived from at least one oil chosen frommarine oil, algae oil, plant-based oil, and microbial oil.
 48. Themethod according to claim 47, wherein the marine oil is a purified fishoil.
 49. The method according to claim 42, wherein the EPA:DHA weightratio of the fatty acid oil mixture ranges from about 1:10 to 10:1. 50.The method according to claim 42, wherein the preconcentrate furthercomprises at least one co-surfactant chosen from short chain alcohols,glycol ethers, pyrrolidine derivatives, 2-pyrrolidone, bile salts, andmixtures thereof.
 51. The method according to claim 42, wherein thepreconcentrate further comprises at least one antioxidant in an amountless than a pharmaceutically effective amount.
 52. The method accordingto claim 42, wherein the preconcentrate is in the form of a gelatincapsule.
 53. The method according to claim 52, wherein the capsule fillcontent ranges from about 0.400 g to about 1.300 g.
 54. The methodaccording to claim 42, wherein the preconcentrate is administered onceper day.
 55. The method according to claim 42, wherein thepreconcentrate forms a self-nanoemulsifying drug delivery system(SNEDDS), self-microemulsifying drug delivery system (SMEDDS), orself-emulsifying drug delivery system (SEDDS) in an aqueous solution.56. A preconcentrate comprising: a fatty acid oil mixture comprisingfrom about 25% to about 75% eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA), by weight of the fatty acid oil mixture,wherein the EPA and DHA are in a form chosen from ethyl ester andtriglyceride; and from about 0.5% to about 40% of at least one nonionicsurfactant chosen from polysorbate 20, polysorbate 80, and mixturesthereof, by weight relative to the total weight of the preconcentrate,wherein the at least one nonionic surfactant enhances lipolysis of EPAand DHA ethyl esters; wherein the preconcentrate does not comprise apharmaceutically active agent other than the fatty acid oil mixture. 57.The preconcentrate according to claim 56, wherein the fatty acid oilmixture comprises from about 35% to about 75% EPA and DHA.
 58. Thepreconcentrate according to claim 56, wherein the fatty acid oil mixtureis derived from at least one oil chosen from marine oil, algae oil,plant-based oil, and microbial oil.
 59. The preconcentrate according toclaim 58, wherein the marine oil is a purified fish oil.
 60. Thepreconcentrate according to claim 56, wherein the EPA:DHA weight ratioof the fatty acid oil mixture ranges from about 1:10 to about 10:1. 61.The preconcentrate according to claim 56, further comprising at leastone co-surfactant chosen from short chain alcohols, glycol ethers,pyrrolidine derivatives, 2-pyrrolidone, bile salts, and mixturesthereof.
 62. The preconcentrate according to claim 56, furthercomprising at least one antioxidant in an amount less than apharmaceutically effective amount.
 63. The preconcentrate according toclaim 56, wherein the preconcentrate is in the form of a gelatincapsule.
 64. The preconcentrate according to claim 63, wherein thecapsule fill content ranges from about 0.400 g to about 1.300 g.
 65. Thepreconcentrate according to claim 56, wherein the preconcentrate forms aself-nanoemulsifying drug delivery system (SNEDDS),self-microemulsifying drug delivery system (SMEDDS), or self-emulsifyingdrug delivery system (SEDDS) in an aqueous solution.
 66. A method forenhancing at least one parameter chosen from hydrolysis, solubility,bioavailability, absorption, and combinations thereof ofeicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) comprisingcombining: a fatty acid oil mixture comprising EPA and DHA in a formchosen from ethyl ester and triglyceride; and at least one nonionicsurfactant chosen from polysorbate 20, polysorbate 80, and mixturesthereof; wherein the fatty acid oil mixture and the at least onenonionic surfactant form a preconcentrate; and wherein thepreconcentrate does not comprise a pharmaceutically active agent otherthan the fatty acid oil mixture.
 67. The method according to claim 66,wherein the fatty acid oil mixture comprises at least 75%eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), by weight ofthe fatty acid oil mixture.
 68. The method according to claim 66,wherein the fatty acid oil mixture comprises from about 25% to about 75%eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), by weight ofthe fatty acid oil mixture.
 69. The method according to claim 66,wherein the preconcentrate further comprises at least one co-surfactantchosen from short chain alcohols, glycol ethers, pyrrolidinederivatives, 2-pyrrolidone, bile salts, and mixtures thereof.
 70. Themethod according to claim 67, wherein the fatty acid oil mixturecomprises from about 80% to about 88% eicosapentaenoic acid (EPA) anddocosahexaenoic acid (DHA), by weight of the fatty acid oil mixture. 71.The method according to claim 70, wherein the preconcentrate furthercomprises at least one co-surfactant comprising ethanol.
 72. The methodaccording to claim 66, wherein the preconcentrate forms aself-nanoemulsifying drug delivery system (SNEDDS),self-microemulsifying drug delivery system (SMEDDS), or self-emulsifyingdrug delivery system (SEDDS) in an aqueous solution.
 73. The methodaccording to claim 72, wherein the system comprises an emulsion with aparticle size ranging from about 150 nm to about 350 nm.
 74. Thepreconcentrate of claim 1, further comprising: at least one free fattyacid chosen from oleic acid and linoleic acid; and at least oneantioxidant in an amount less than a pharmaceutically effective amount.75. The preconcentrate of claim 74, wherein: the fatty acid oil mixturecomprises about 84% EPA and DHA, by weight of the fatty acid oilmixture; the at least one nonionic surfactant comprises polysorbate 20;and the at least one free fatty acid comprises oleic acid.
 76. Thepreconcentrate of claim 1, wherein the preconcentrate further comprisesat least one co-surfactant chosen from short chain alcohols.
 77. Thepreconcentrate of claim 56, wherein the preconcentrate further comprisesat least one co-surfactant chosen from short chain alcohols.
 78. Thepreconcentrate of claim 56, further comprising: at least one free fattyacid chosen from oleic acid and linoleic acid; and at least oneantioxidant in an amount less than a pharmaceutically effective amount.79. The preconcentrate of claim 78, wherein: the at least one nonionicsurfactant comprises polysorbate 20; and the at least one free fattyacid comprises oleic acid.
 80. The preconcentrate according to claim 56,wherein the fatty acid oil mixture further comprises at least one otherfatty acid other than EPA and DHA chosen from α-linolenic acid (ALA),heneicosapentaenoic acid (HPA), docosapentaenoic acid (DPA),eicosatetraenoic acid (ETA), eicosatrienoic acid (ETE), stearidonic acid(STA), linoleic acid, gamma-linolenic acid (GLA), arachidonic acid (AA),osbond acid, and mixtures thereof.
 81. The preconcentrate according toclaim 56, wherein the fatty acid oil mixture comprises at least oneother fatty acid other than EPA and DHA chosen from oleic acid,ricinoleic acid, erucic acid, and mixtures thereof.
 82. Thepreconcentrate according to claim 1, wherein the fatty acid oil mixturecomprises at least one other fatty acid other than EPA and DHA chosenfrom oleic acid, ricinoleic acid, erucic acid, and mixtures thereof. 83.The preconcentrate according to claim 23, wherein the fatty acid oilmixture comprises at least one other fatty acid other than EPA and DHAchosen from oleic acid, ricinoleic acid, erucic acid, and mixturesthereof.
 84. The preconcentrate according to claim 42, wherein the fattyacid oil mixture comprises at least one other fatty acid other than EPAand DHA chosen from oleic acid, ricinoleic acid, erucic acid, andmixtures.
 85. The preconcentrate according to claim 1, wherein theEPA:DHA weight ratio of the fatty acid oil mixture ranges from about 1:6to 6:1.
 86. The preconcentrate according to claim 1, wherein the EPA:DHAweight ratio of the fatty acid oil mixture ranges from about 1:3 to 3:1.87. The preconcentrate according to claim 1, wherein the EPA:DHA weightratio of the fatty acid oil mixture ranges from about 1:2 to 1:3. 88.The preconcentrate according to claim 1, wherein the preconcentratecomprises from about 10% to about 25% of the at least one nonionicsurfactant, by weight relative to the total weight of thepreconcentrate.
 89. The preconcentrate according to claim 1, wherein theweight ratio of fatty acid oil mixture:total surfactant ranges fromabout 1:1 to about 50:1.
 90. The preconcentrate according to claim 1,wherein the weight ratio of fatty acid oil mixture:total surfactantranges from about 1:1 to 6:1.
 91. The preconcentrate according to claim1, wherein the weight ratio of fatty acid oil mixture:total surfactantranges from about 1:1 to about 3:1.
 92. The preconcentrate according toclaim 19, wherein the capsule fill content ranges from about 0.600 g toabout 1.200 g.
 93. The preconcentrate according to claim 19, wherein thecapsule fill content ranges from about 0.800 g to about 1.000 g.
 94. Thesystem according to claim 23, wherein the EPA:DHA weight ratio of thefatty acid oil mixture ranges from about 1:6 to 6:1.
 95. The systemaccording to claim 23, wherein the EPA:DHA weight ratio of the fattyacid oil mixture ranges from about 1:3 to 3:1.
 96. The system accordingto claim 23, wherein the EPA:DHA weight ratio of the fatty acid oilmixture ranges from about 1:2 to 1:3.
 97. The system according to claim23, wherein the preconcentrate comprises from about 10% to about 25% ofthe at least one nonionic surfactant, by weight relative to the totalweight of the preconcentrate.
 98. The system according to claim 23,wherein the weight ratio of fatty acid oil mixture:total surfactantranges from about 1:1 to about 50:1.
 99. The system according to claim23, wherein the weight ratio of fatty acid oil mixture:total surfactantranges from about 1:1 to 6:1.
 100. The system according to claim 23,wherein the weight ratio of fatty acid oil mixture:total surfactantranges from about 1:1 to about 3:1.
 101. The system according to claim39, wherein the capsule fill content ranges from about 0.600 g to about1.200 g.
 102. The system according to claim 39, wherein the capsule fillcontent ranges from about 0.800 g to about 1.000 g.
 103. The methodaccording to claim 42, wherein the EPA:DHA weight ratio of the fattyacid oil mixture ranges from about 1:6 to 6:1.
 104. The method accordingto claim 42, wherein the EPA:DHA weight ratio of the fatty acid oilmixture ranges from about 1:3 to 3:1.
 105. The method according to claim42, wherein the EPA:DHA weight ratio of the fatty acid oil mixtureranges from about 1:2 to 1:3.
 106. The method according to claim 52,wherein the capsule fill content ranges from about 0.600 g to about1.200 g.
 107. The method according to claim 52, wherein the capsule fillcontent ranges from about 0.800 g to about 1.000 g.
 108. The methodaccording to claim 42, wherein the preconcentrate is administered twiceper day.
 109. The method according to claim 42, wherein thepreconcentrate is administered three times per day.
 110. Thepreconcentrate according to claim 56, wherein the fatty acid oil mixturecomprises from about 40% to about 70% EPA and DHA, by weight of thefatty acid oil mixture.
 111. The preconcentrate according to claim 56,wherein the fatty acid oil mixture comprises from about 40% to about 60%EPA and DHA, by weight of the fatty acid oil mixture.
 112. Thepreconcentrate according to claim 56, wherein the fatty acid oil mixturecomprises from about 40% to about 55% EPA and DHA, by weight of thefatty acid oil mixture.
 113. The preconcentrate according to claim 56,wherein the fatty acid oil mixture comprises from about 50% to about 55%EPA and DHA, by weight of the fatty acid oil mixture.
 114. Thepreconcentrate according to claim 56, wherein the EPA:DHA weight ratioof the fatty acid oil mixture ranges from about 1:6 to 6:1.
 115. Thepreconcentrate according to claim 56, wherein the EPA:DHA weight ratioof the fatty acid oil mixture ranges from about 1:3 to 3:1.
 116. Thepreconcentrate according to claim 56, wherein the EPA:DHA weight ratioof the fatty acid oil mixture ranges from about 1:2 to 1:3.
 117. Thepreconcentrate according to claim 63, wherein the capsule fill contentranges from about 0.600 g to about 1.200 g.
 118. The preconcentrateaccording to claim 63, wherein the capsule fill content ranges fromabout 0.800 g to about 1.000 g.
 119. The preconcentrate according toclaim 56, wherein the preconcentrate is a food supplement or nutritionalsupplement.